1572-08-3

Usage

Structure

Linear chain with a hydroxyl group (OH) and a double bond between the second and third carbon atoms

Physical state

Colorless liquid

Uses

Synthesis of various organic compounds, flavoring agent in the food industry, production of perfumes and fragrances, chemical intermediate in manufacturing of pharmaceuticals and agricultural products

Aroma

Pleasant

Upstream product

• 54716-03-9 3-methylpenta-2(Z),4-dien-1-al 
• 40930-20-9 (2Z)-3-methylpenta-2,4-dien-1-ol 

Downstream Products

• 75420-45-0 (S)-(+)-3-methyl-4-penten-1-ol 
• 123502-30-7 (E)-3-methyl-5-benzyloxy-1,3-pentadiene 
• 123502-37-4 (4aR,5R,8aR)-5-Benzyloxymethyl-4a-methoxymethoxymethyl-1,1,6-trimethyl-1,2,3,4,4a,5,8,8a-octahydro-naphthalene 
• 123502-42-1 3-Methoxy-5-methyl-2-((3R,3aR,6aR,10aR)-4,7,7-trimethyl-3,3a,6,6a,7,8,9,10-octahydro-2-oxa-cyclopenta[d]naphthalen-3-yl)-phenol 
• 123502-35-2 (1S,4aR,8R,8aS)-8-Benzyloxymethyl-8a-methoxymethoxymethyl-4,4,7-trimethyl-1,2,3,4,4a,5,8,8a-octahydro-naphthalen-1-ol 
• 123502-41-0 (3R,3aR,6aR,10aR)-3-(2,6-Dimethoxy-4-methyl-phenyl)-4,7,7-trimethyl-3,3a,6,6a,7,8,9,10-octahydro-2-oxa-cyclopenta[d]naphthalene 
• 123502-31-8 (4aR,5R,8aR)-5-Benzyloxymethyl-1,1,6-trimethyl-4-oxo-1,5,8,8a-tetrahydro-4H-naphthalene-4a-carboxylic acid methyl ester 
• 123502-33-0 (4aR,5R,8aR)-5-Benzyloxymethyl-1,1,6-trimethyl-4-oxo-1,3,4,5,8,8a-hexahydro-2H-naphthalene-4a-carboxylic acid methyl ester 
• 123502-40-9 (2,6-Dimethoxy-4-methyl-phenyl)-((1S,4aS,8aS)-8a-methoxymethoxymethyl-2,5,5-trimethyl-1,4,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-methanol 
• 123502-36-3 Dithiocarbonic acid O-((1S,4aR,8R,8aS)-8-benzyloxymethyl-8a-methoxymethoxymethyl-4,4,7-trimethyl-1,2,3,4,4a,5,8,8a-octahydro-naphthalen-1-yl) ester S-methyl ester 
• 123502-32-9 (4aS,5S,8aS)-5-Benzyloxymethyl-1,1,6-trimethyl-4-triethylsilanyloxy-1,5,8,8a-tetrahydro-2H-naphthalene-4a-carboxylic acid methyl ester 
• 17909-77-2 (E,E,E)-2,6,10-trimethyl-2,6,9,11-dodecatetraenal 
• 3779-61-1 trans ocimene 
• 98066-12-7 (+/-)-(E)-7-<<(3-tetrahydro-5,5-dimethyl-4-oxo-2-furanyl)-2-butenyl>-oxy>-2H-1-benzopyran-2-one 

Relevant academic research and scientific papers

REGIO- AND STEREOSELECTIVE HYDROGENATION OF METHYL SUBSTITUTED PENTADIEN-1-OLS BY BAKER'S YEAST

(E)-2-methyl and (E)-3-methyl-2,4-pentadien-1-ols are reduced to (S)-2-methyl- and (S)-3-methyl-4-penten-1-ols, respectively, using baker's yeast as a regio- and stereoselective reagent.This microbiological conversion provides an efficient route to bifunctional and enantiomerically pure C6-building blocks containing the C'-CH(Me)-C'' grouping.